Variant report

Variant	nsv900257
Chromosome Location	chr13:62782367-62907090
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:570)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:570 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:62894405-62894638	HepG2	liver:	n/a	n/a
2	ATF2	chr13:62783484-62784127	GM12878	blood:	n/a	n/a
3	ATF2	chr13:62783598-62784160	GM12878	blood:	n/a	n/a
4	BATF	chr13:62783637-62783935	GM12878	blood:	n/a	n/a
5	BATF	chr13:62867251-62867539	GM12878	blood:	n/a	n/a
6	BATF	chr13:62782112-62782384	GM12878	blood:	n/a	n/a
7	BCL11A	chr13:62783559-62784083	GM12878	blood:	n/a	n/a
8	BCL11A	chr13:62783637-62783901	GM12878	blood:	n/a	n/a
9	BCL11A	chr13:62884071-62884344	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCLAF1	chr13:62783584-62784098	GM12878	blood:	n/a	n/a
11	BCLAF1	chr13:62879889-62880316	GM12878	blood:	n/a	chr13:62880047-62880056
12	BHLHE40	chr13:62783623-62784081	GM12878	blood:	n/a	n/a
13	BHLHE40	chr13:62894337-62894537	GM12878	blood:	n/a	n/a
14	BRCA1	chr13:62854907-62854933	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr13:62904739-62904877	H1-hESC	embryonic stem cell:	n/a	chr13:62904793-62904804
16	CEBPB	chr13:62817082-62817383	HepG2	liver:	n/a	n/a
17	CEBPB	chr13:62817048-62817878	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr13:62817015-62817503	MCF-7	breast:	n/a	n/a
19	CEBPB	chr13:62868302-62868867	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr13:62824670-62825455	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr13:62817127-62817378	A549	lung:	n/a	n/a
22	CEBPB	chr13:62783490-62784154	GM12878	blood:	n/a	n/a
23	CEBPB	chr13:62904583-62904971	IMR90	lung:	n/a	chr13:62904793-62904804
24	CEBPB	chr13:62884605-62885021	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr13:62784246-62784460	HepG2	liver:	n/a	chr13:62784370-62784381 chr13:62784356-62784369 chr13:62784356-62784367 chr13:62784356-62784369
26	CEBPB	chr13:62817129-62817512	MCF-7	breast:	n/a	n/a
27	CEBPB	chr13:62868403-62868741	IMR90	lung:	n/a	n/a
28	CEBPB	chr13:62784218-62784418	K562	blood:	n/a	chr13:62784370-62784381 chr13:62784356-62784369 chr13:62784356-62784367 chr13:62784356-62784369
29	CEBPB	chr13:62904679-62904958	HepG2	liver:	n/a	chr13:62904793-62904804
30	CEBPB	chr13:62817085-62817392	IMR90	lung:	n/a	n/a
31	CEBPB	chr13:62867010-62867649	Hela-S3	cervix:	n/a	n/a
32	CHD1	chr13:62783582-62784020	GM12878	blood:	n/a	n/a
33	CHD1	chr13:62894450-62894587	GM12878	blood:	n/a	n/a
34	CHD2	chr13:62867277-62867517	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr13:62783476-62784129	GM12878	blood:	n/a	n/a
36	CHD2	chr13:62884047-62884436	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr13:62783299-62784150	GM12878	blood:	n/a	chr13:62783676-62783689
38	CTCF	chr13:62894360-62894510	AG04450	lung:	n/a	chr13:62894443-62894464 chr13:62894441-62894459
39	CTCF	chr13:62894400-62894550	GM12801	blood:	n/a	chr13:62894443-62894464 chr13:62894441-62894459
40	CTCF	chr13:62894340-62894490	HCFaa	heart:	n/a	chr13:62894443-62894464 chr13:62894441-62894459
41	CTCF	chr13:62894422-62894499	MCF-7	breast:	n/a	chr13:62894443-62894464 chr13:62894441-62894459
42	CTCF	chr13:62786520-62786670	HepG2	liver:	n/a	n/a
43	CTCF	chr13:62786500-62786650	GM12874	blood:	n/a	n/a
44	CTCF	chr13:62819145-62819194	LNCaP	prostate:	n/a	n/a
45	CTCF	chr13:62894365-62894508	HepG2	liver:	n/a	chr13:62894443-62894464 chr13:62894441-62894459
46	CTCF	chr13:62895580-62895730	HPF	lung:	n/a	n/a
47	CTCF	chr13:62894367-62894537	GM10266	blood:	n/a	chr13:62894443-62894464 chr13:62894441-62894459
48	CTCF	chr13:62894360-62894510	RPTEC	kidney:	n/a	chr13:62894443-62894464 chr13:62894441-62894459
49	CTCF	chr13:62894400-62894550	HPAF	blood vessel:	n/a	chr13:62894443-62894464 chr13:62894441-62894459
50	CTCF	chr13:62852420-62852570	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:62884315-62884365	HRPEpiC	eye:	n/a
2	chr13:62884315-62884365	ovcar-3	ovarian:	n/a
3	chr13:62884315-62884365	AoSMC	blood vessel:	n/a
4	chr13:62884315-62884365	AG09319	gingival:	n/a
5	chr13:62884315-62884365	AG09309	skin:	n/a
6	chr13:62884315-62884365	LNCaP	prostate:	n/a
7	chr13:62884315-62884365	HRE	kidney:	n/a
8	chr13:62884315-62884365	GM12892	blood:	n/a
9	chr13:62884315-62884365	NT2-D1	testis:	n/a
10	chr13:62884315-62884365	A549	lung:	n/a
11	chr13:62884315-62884365	HCPEpiC	choroid plexus:	n/a
12	chr13:62884315-62884365	HL-60	blood:	n/a
13	chr13:62884315-62884365	RPTEC	kidney:	n/a
14	chr13:62884315-62884365	SAEC	small airway:	n/a
15	chr13:62884315-62884365	HEEpiC	esophagus:	n/a
16	chr13:62884315-62884365	MCF-7	breast:	n/a
17	chr13:62884315-62884365	NB4	blood:	n/a
18	chr13:62884315-62884365	SK-N-SH	brain:	n/a
19	chr13:62884315-62884365	Hepatocyte	liver:	n/a
20	chr13:62884315-62884365	HAEpiC	amniotic membrane:	n/a
21	chr13:62884315-62884365	SKMC	muscle:	n/a
22	chr13:62884315-62884365	HEK293	kidney:	embryo
23	chr13:62884315-62884365	CMK	blood:	n/a
24	chr13:62884315-62884365	AG04450	lung:	fetal
25	chr13:62884315-62884365	HCM	heart:	n/a
26	chr13:62884315-62884365	K562	blood:	n/a
27	chr13:62884315-62884365	NH-A	brain:	n/a
28	chr13:62884315-62884365	T-47D	breast:	n/a
29	chr13:62884315-62884365	AG04449	skin:	fetal
30	chr13:62884315-62884365	GM12878	blood:	n/a
31	chr13:62884315-62884365	H1-hESC	embryonic stem cell:	embryo
32	chr13:62884315-62884365	HepG2	liver:	n/a
33	chr13:62884315-62884365	HNPCEpiC	eye:	n/a
34	chr13:62884315-62884365	GM12891	blood:	n/a
35	chr13:62884315-62884365	Jurkat	blood:	n/a
36	chr13:62884315-62884365	IMR90	lung:	fetal
37	chr13:62884315-62884365	BJ	skin:	n/a
38	chr13:62884315-62884365	HMEC	breast:	n/a
39	chr13:62884315-62884365	HPAEpiC	pulmonary alveolar:	n/a
40	chr13:62884315-62884365	GM06990	blood:	n/a
41	chr13:62884315-62884365	BE2_C	brain:	n/a
42	chr13:62884315-62884365	U87	brain:	n/a
43	chr13:62884315-62884365	PANC-1	pancreas:	n/a
44	chr13:62884315-62884365	HCT-116	colon:	n/a
45	chr13:62884315-62884365	HRCEpiC	kidney:	n/a
46	chr13:62884315-62884365	Hela-S3	cervix:	n/a
47	chr13:62884315-62884365	NHDF-neo	bronchial:	n/a
48	chr13:62884315-62884365	HCF	heart:	n/a
49	chr13:62884315-62884365	ECC-1	luminal epithelium:	n/a
50	chr13:62884315-62884365	SK-N-SH_RA	brain:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:62693885..62694482-chr13:62894021..62894947,2	MCF-7	breast:
2	chr13:62805513..62806033-chr5:25238045..25239045,2	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL445989.1-7	chr13:62801767-62801865	XLOC_010407
2	lnc-AL445989.1-25	chr13:62902121-62902517	NONHSAT034144
3	lnc-AL445989.1-7	chr13:62798229-62798327	NONHSAT034140
4	lnc-AL445989.1-7	chr13:62801767-62801865	XLOC_010407
5	lnc-AL445989.1-7	chr13:62823960-62824080	XLOC_010407
6	lnc-AL445989.1-5	chr13:62897790-62898087	ENSG00000229307.1
7	lnc-AL445989.1-7	chr13:62807277-62807564	NONHSAT034140
8	lnc-AL445989.1-6	chr13:62895438-62895519	XLOC_010408
9	lnc-AL445989.1-7	chr13:62801766-62801865	NONHSAT034140
10	lnc-AL445989.1-6	chr13:62896059-62896531	XLOC_010408
11	lnc-AL445989.1-7	chr13:62807278-62807564	XLOC_010407
12	lnc-AL445989.1-7	chr13:62798240-62798327	XLOC_010407
13	lnc-AL445989.1-7	chr13:62823959-62824080	NONHSAT034140
14	lnc-AL445989.1-7	chr13:62798230-62798327	XLOC_010407
15	lnc-AL445989.1-5	chr13:62902889-62902966	ENSG00000229307.1

No data

Variant related genes	Relation type
LINC01075	TF binding region
RPL32P28	TF binding region
LINC01074	TF binding region
LINC00459	TF binding region
LINC01075	CpG island
RPL32P28	CpG island
LINC01074	CpG island
LINC00459	CpG island

Extended variants
information (count: 1744 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1744 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7983039	chr13:62782367-62782368	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566606556	chr13:62782398-62782399	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs35900363	chr13:62782421-62782422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556974071	chr13:62782422-62782423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570110723	chr13:62782442-62782443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534697301	chr13:62782452-62782453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs143763790	chr13:62782480-62782481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577729471	chr13:62782483-62782484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs191071	chr13:62782487-62782488	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs138313008	chr13:62782504-62782505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs199515921	chr13:62782515-62782516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs398098896	chr13:62782516-62782517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7987611	chr13:62782527-62782528	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs186152891	chr13:62782538-62782539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs35080151	chr13:62782600-62782601	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs373814215	chr13:62782645-62782646	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs7989138	chr13:62782675-62782676	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs73489953	chr13:62782719-62782720	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs543308856	chr13:62782734-62782735	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs142892286	chr13:62782754-62782755	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs7988008	chr13:62782772-62782773	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs577106093	chr13:62782794-62782795	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs192024636	chr13:62782842-62782843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs9539453	chr13:62782850-62782851	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs111760405	chr13:62782889-62782890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs182781092	chr13:62782967-62782968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs111720750	chr13:62782981-62782982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73219756	chr13:62783018-62783019	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs9539454	chr13:62783031-62783032	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs9539455	chr13:62783081-62783082	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs138827916	chr13:62783099-62783100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs567251442	chr13:62783109-62783110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs114706995	chr13:62783129-62783130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs115449306	chr13:62783132-62783133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs141978741	chr13:62783181-62783182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575608916	chr13:62783182-62783183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191374101	chr13:62783223-62783224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs9317229	chr13:62783296-62783297	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs374014986	chr13:62783304-62783305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs66824322	chr13:62783421-62783422	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs35745704	chr13:62783423-62783424	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs397977848	chr13:62783431-62783432	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs540914488	chr13:62783440-62783441	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs187179815	chr13:62783523-62783524	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs376425363	chr13:62783527-62783528	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs543818192	chr13:62783529-62783530	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs369178676	chr13:62783558-62783559	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs373292852	chr13:62783565-62783566	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs529724791	chr13:62783566-62783567	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs34744626	chr13:62783650-62783651	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Anaplastic thyroid cancer	18753363	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:62781600-62782400	ZNF genes & repeats	GM12878-XiMat	blood
2	chr13:62782400-62782600	Enhancers	GM12878-XiMat	blood
3	chr13:62782600-62782800	Flanking Active TSS	GM12878-XiMat	blood
4	chr13:62782800-62783400	Enhancers	GM12878-XiMat	blood
5	chr13:62783400-62783600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr13:62783400-62783800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr13:62783400-62783800	Flanking Active TSS	GM12878-XiMat	blood
8	chr13:62783400-62784000	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr13:62783600-62784000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr13:62783600-62784000	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr13:62783600-62784200	Active TSS	Hela-S3	cervix
12	chr13:62783800-62784200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr13:62783800-62784200	Active TSS	GM12878-XiMat	blood
14	chr13:62784000-62784200	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr13:62784200-62785000	Enhancers	GM12878-XiMat	blood
16	chr13:62798600-62799000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr13:62799200-62799600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr13:62806000-62806400	Enhancers	GM12878-XiMat	blood
19	chr13:62809200-62811200	Enhancers	Fetal Lung	lung
20	chr13:62817600-62818000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr13:62818000-62824000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr13:62824000-62826200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr13:62824400-62825600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr13:62824600-62825200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr13:62824600-62825200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr13:62824600-62826000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr13:62824800-62825400	Enhancers	Hela-S3	cervix
28	chr13:62825200-62832600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr13:62830200-62830400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr13:62832600-62832800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr13:62847800-62849000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr13:62849000-62849800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr13:62849800-62850000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr13:62850000-62850600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr13:62850000-62850800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr13:62850600-62850800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr13:62850800-62851400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr13:62858000-62858400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr13:62863400-62864600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr13:62863600-62864600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr13:62867000-62867400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr13:62867000-62867600	Enhancers	Muscle Satellite Cultured Cells	--
43	chr13:62867000-62867800	Enhancers	GM12878-XiMat	blood
44	chr13:62867000-62868000	Enhancers	Hela-S3	cervix
45	chr13:62867400-62867600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr13:62867600-62868600	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr13:62867800-62870600	Weak transcription	GM12878-XiMat	blood
48	chr13:62868000-62868400	Weak transcription	Hela-S3	cervix
49	chr13:62868400-62868800	Enhancers	Hela-S3	cervix
50	chr13:62868600-62869000	Enhancers	Muscle Satellite Cultured Cells	--

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